scholarly journals Purification, crystallization and preliminary X-ray diffraction analysis of DNA damage response A protein fromDeinococcus radiodurans

Author(s):  
Mitsugu Yamada ◽  
Katsuya Satoh ◽  
Issay Narumi
2014 ◽  
Vol 9 (1) ◽  
pp. 169-176 ◽  
Author(s):  
YANG JIAO ◽  
CHANG LIU ◽  
FENG-MEI CUI ◽  
JIA-YING XU ◽  
JIAN TONG ◽  
...  

2017 ◽  
Vol 58 (1) ◽  
pp. 59-65 ◽  
Author(s):  
Yudai Izumi ◽  
Kentaro Fujii ◽  
Satoshi Yamamoto ◽  
Koichi Matsuo ◽  
Hirofumi Namatame ◽  
...  

Abstract Synchrotron-radiation circular-dichroism spectroscopy was used to reveal that the DNA damage response induces a decrement of α-helix and an increment of β-strand contents of histone H3–H4 extracted from X-ray–irradiated human HeLa cells. The trend of the structural alteration was qualitatively opposite to that of our previously reported results for histone H2A–H2B. These results strongly suggest that histones share roles in DNA damage responses, particularly in DNA repair processes and chromatin remodeling, via a specific structural alteration of each histone.


Biomedicines ◽  
2021 ◽  
Vol 9 (10) ◽  
pp. 1473
Author(s):  
Xiang-Zhong Liu ◽  
Mi Zhou ◽  
Chun-Chun Du ◽  
Hong-Hong Zhu ◽  
Xi Lu ◽  
...  

(±)-Hypersines A–C (1–3), the three pairs of enantiomerically pure monoterpenoid polyprenylated acylphloroglucinols with an unprecedented 6/6/5/4 fused ring system, were isolated from Hypericum elodeoides. Their structures, including absolute configurations, were elucidated by comprehensive spectroscopic data, single-crystal X-ray diffraction, and quantum chemical calculations. The plausible, biosynthetic pathway of 1–3 was proposed. Moreover, the bioactivity evaluation indicated that 1a might be a novel DNA damage response inhibitor, and could enhance MCF-7 cell sensitivity to the anticancer agent, camptothecin.


Author(s):  
Dong Li ◽  
Ying Ge ◽  
Ze Zhao ◽  
Rui Zhu ◽  
Xiang Wang ◽  
...  

Small non-coding RNAs (ncRNAs), including microRNAs (miRNAs) and PIWI-interacting RNAs (piRNAs), play a pivotal role in biological processes. A comprehensive quantitative reference of small ncRNAs expression during development and in DNA damage response (DDR) would significantly advance our understanding of their roles. In this study, we systemically analyzed the expression profile of miRNAs and piRNAs in wild-type flies, e2f1 mutant, p53 mutant and e2f1 p53 double mutant during development and after X-ray irradiation. By using small RNA sequencing and bioinformatic analysis, we found that both miRNAs and piRNAs were expressed in a dynamic mode and formed 4 distinct clusters during development. Notably, the expression pattern of miRNAs and piRNAs was changed in e2f1 mutant at multiple developmental stages, while retained in p53 mutant, indicating a critical role of E2f1 played in mediating small ncRNAs expression. Moreover, we identified differentially expressed (DE) small ncRNAs in e2f1 mutant and p53 mutant after X-ray irradiation. Furthermore, we mapped the binding motif of E2f1 and p53 around the small ncRNAs. Our data suggested that E2f1 and p53 work differently yet coordinately to regulate small ncRNAs expression, and E2f1 may play a major role to regulate miRNAs during development and after X-ray irradiation. Collectively, our results provide comprehensive characterization of small ncRNAs, as well as the regulatory roles of E2f1 and p53 in small ncRNAs expression, during development and in DNA damage response, which reveal new insights into the small ncRNAs biology.


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